Variant report

Variant rs12457641
Chromosome Location chr18:30337905-30337906
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:30333800-30341400 Weak transcription Fetal Kidney kidney
2 chr18:30334200-30338800 Weak transcription Dnd41 blood
3 chr18:30335200-30339600 Weak transcription H1 Cell Line embryonic stem cell
4 chr18:30335200-30340000 Weak transcription Fetal Brain Male brain
5 chr18:30335200-30340400 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr18:30335600-30339800 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr18:30335600-30342200 Enhancers Primary B cells from peripheral blood blood
8 chr18:30335800-30339600 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr18:30336000-30339600 Weak transcription HUES48 Cell Line embryonic stem cell
10 chr18:30336200-30339400 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr18:30336200-30339600 Weak transcription iPS-20b Cell Line embryonic stem cell
12 chr18:30336200-30339800 Genic enhancers Primary B cells from cord blood blood
13 chr18:30336400-30338400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr18:30337400-30339600 Strong transcription HepG2 liver
15 chr18:30337600-30339800 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr18:30337800-30338200 Enhancers Fetal Heart heart
17 chr18:30337800-30339400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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